Ankita Patel

18.6k citations

143 papers · 6.5k · 1 hit paper · h-index 42

Impact in

Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders

Papers in

Genetics 94
- Genomic variations and chromosomal abnormalities 81
- Genomics and Rare Diseases 19
- Genetics and Neurodevelopmental Disorders 17
Molecular Biology 54
- Congenital heart defects research 26

Co-authors: Sau Wai Cheung (66 shared papers)James R. Lupski (33 shared papers)Chad A. Shaw (27 shared papers)Paweł Stankiewicz (35 shared papers)Arthur L. Beaudet (22 shared papers)Carlos A. Bacino (26 shared papers)A. Craig Chinault (17 shared papers)Constance A. Griffin (3 shared papers)
Journals: European Journal of Human Genetics (10 papers)Genetics in Medicine (10 papers)Prenatal Diagnosis (4 papers)PLoS Genetics (4 papers)American Journal of Medical Genetics Part A (27 papers)
Partner nations: United States India Canada

In The Last Decade

Ankita Patel

135 papers receiving 6.3k citations

Ankita Patel's Hit Papers

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Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) 2019 · 879 citations

Peers

Countries citing papers authored by Ankita Patel

Since Specialization

Citations

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Fields of papers citing papers by Ankita Patel

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Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ankita Patel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ankita Patel. The network helps show where Ankita Patel may publish in the future.

Co-authors

The 25 scholars most cited alongside Ankita Patel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ankita Patel Line = papers co-authored together Ankita Patel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 143 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) Genetics in Medicine ·Erin Rooney Riggs, Erica Andersen, Athena M. Cherry, Sibel Kantarci, Hutton M. Kearney, Ankita Patel, Gordana Raca, Deborah Ritter, Sarah T. South, Erik C. Thorland, Daniel Pineda‐Alvarez, Swaroop Aradhya, Alastair J. Martin Hit paper breakdown →	2019	879
2	ALK1 and p80 Expression and Chromosomal Rearrangements Involving 2p23 in Inflammatory Myofibroblastic Tumor Modern Pathology ·Cheryl M. Coffin, Ankita Patel, Sherrie L. Perkins, Kojo S.J. Elenitoba‐Johnson, Elizabeth J. Perlman, Constance A. Griffin	2001	450
3	SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties Nature ·Kihoon Han, J. Lloyd Holder, Christian P. Schaaf, Hui Lü, Hongmei Chen, Hyojin Kang, Jianrong Tang, Zhenyu Wu, Shuang Hao, Sau Wai Cheung, Peng Yu, Hao Sun, Amy M. Breman, Ankita Patel, Hui‐Chen Lu, Huda Y. Zoghbi	2013	280
4	Development and validation of a CGH microarray for clinical cytogenetic diagnosis Genetics in Medicine ·Sau Wai Cheung, Chad A. Shaw, Wei Yu, Jiangzham Li, Zhishuo Ou, Ankita Patel, Svetlana A. Yatsenko, M. Lance Cooper, Patti Furman, P Stankiewicz, James R. Lupski, A. Craig Chinault, Arthur L. Beaudet	2005	185
5	Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia Nature Genetics ·Xiaoling Wang, V. Reid Sutton, J Omar Peraza-Llanes, Zhiyin Yu, Rebecca Rosetta, Ying-Chuck Kou, Tanya N. Eble, Ankita Patel, Christina Thaller, Ping Fang, Ignatia B. Van den Veyver	2007	178
6	Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases Prenatal Diagnosis ·Ignatia B. Van den Veyver, Ankita Patel, Chad A. Shaw, Amber N. Pursley, Sung‐Hae Kang, Marcia J. Simovich, Patricia A. Ward, Sandra Darilek, Anthony E. Johnson, Sarah E. Neill, Weimin Bi, Lisa D. White, Christine M. Eng, James R. Lupski, Sau Wai Cheung, Arthur L. Beaudet	2008	155
7	USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder Molecular Cell ·Yi-Heng Hao, Michael D. Fountain, Klementina Fon Tacer, Fan Xia, Weimin Bi, Sung‐Hae Kang, Ankita Patel, Jill A. Rosenfeld, Cédric Le Caignec, Bertrand Isidor, Ian D. Krantz, Sarah E. Noon, Jean P. Pfotenhauer, Thomas M. Morgan, Rocio Moran, Robert C. Pedersen, Margarita Sáenz, Christian P. Schaaf, Patrick Ryan Potts	2015	149
8	Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases PLoS ONE ·Xinyan Lu, Chad A. Shaw, Ankita Patel, Jiangzhen Li, M. Lance Cooper, William R. Wells, Cathy Sullivan, Trilochan Sahoo, Svetlana A. Yatsenko, Carlos A. Bacino, Paweł Stankiewicz, Zhishu Ou, A. Craig Chinault, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung, Patricia A. Ward	2007	147
9	Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching Human Molecular Genetics ·Claudia M.B. Carvalho, Feng Zhang, Pengfei Liu, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Chad A. Shaw, Sandra Peacock, Amber N. Pursley, Y. Jane Tavyev, Melissa B. Ramocki, Magdalena Nawara, Ewa Obersztyn, Angela Maria Vianna‐Morgante, Paweł Stankiewicz, Huda Y. Zoghbi, Sau Wai Cheung, James R. Lupski	2009	146
10	22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome The American Journal of Human Genetics ·Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, John W. Belmont, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan S. Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau Wai Cheung, James R. Lupski, Ankita Patel	2008	142
11	A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes Nature Genetics ·Marwan Shinawi, Christian P. Schaaf, Samarth Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan C. Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel, LaDonna Immken, Gayle Patel, Jennifer R. German, Arthur L. Beaudet, Paweł Stankiewicz	2009	141
12	Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics American Journal of Medical Genetics Part A ·Sau Wai Cheung, Chad A. Shaw, Daryl A. Scott, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Amber N. Pursley, Jiangzhen Li, Robert P. Erickson, Andrea Gropman, David T. Miller, Margretta R. Seashore, Anne Summers, Paweł Stankiewicz, A. Craig Chinault, James R. Lupski, Arthur L. Beaudet, V. Reid Sutton	2007	140
13	Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes Genetics in Medicine ·Zhishuo Ou, Jonathan S. Berg, Hagith Yonath, Victoria B. Enciso, David T. Miller, Jonathan Picker, Tiffanee Lenzi, Catherine E. Keegan, V. Reid Sutton, John W. Belmont, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Elizabeth Roeder, Ankita Patel	2008	139
14	Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization Genetics in Medicine ·Trilochan Sahoo, Sau Wai Cheung, Patricia A. Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L. Kang, Seema R. Lalani, Jiangzhen Li, Sallie McAdoo, Audrey Burke, Chad A. Shaw, Paweł Stankiewicz, A. Craig Chinault, Ignatia B. Van den Veyver, Benjamin B. Roa, Arthur L. Beaudet, Christine M. Eng	2006	128
15	Overexpression of EMS1/cortactin in NIH3T3 fibroblasts causes increased cell motility and invasion in vitro Oncogene ·Ankita Patel, Gary L. Schechter, William J. Wasilenko, Kenneth D. Somers	1998	126
16	Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis PEDIATRICS ·Xin-Yan Lu, My Thao Phung, Chad A. Shaw, Kim Pham, Sarah Neil‐Sztramko, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Paweł Stankiewicz, Sung-Hae L. Kang, Seema R. Lalani, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Arthur L. Beaudet	2008	104
17	Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological? Human Mutation ·Przemysław Szafrański, Christian P. Schaaf, Richard Person, Ian B. Gibson, Zhilian Xia, Sangeetha Mahadevan, Joanna Wiszniewska, Carlos A. Bacino, Seema R. Lalani, Lorraine Potocki, Sung-Hae L. Kang, Ankita Patel, Sau Wai Cheung, Frank J. Probst, Brett H. Graham, Marwan Shinawi, Arthur L. Beaudet, Paweł Stankiewicz	2010	94
18	Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases American Journal of Medical Genetics Part A ·Lina Shao, Chad A. Shaw, Xinyan Lu, Trilochan Sahoo, Carlos A. Bacino, Seema R. Lalani, Paweł Stankiewicz, Svetlana A. Yatsenko, Yinfeng Li, Sarah E. Neill, Amber N. Pursley, A. Craig Chinault, Ankita Patel, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung	2008	92
19	Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature Prenatal Diagnosis ·Amy M. Breman, Amber N. Pursley, Patricia Hixson, Weimin Bi, Patricia A. Ward, Carlos A. Bacino, Chad A. Shaw, James R. Lupski, Arthur L. Beaudet, Ankita Patel, Sau Wai Cheung, Ignatia Van den Veyver	2012	89
20	Phenotypic manifestations of copy number variation in chromosome 16p13.11 European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani, Ayelet Erez, Patricia I. Bader, Seema R. Lalani, Daryl A. Scott, Fernando Scaglia, Sharon E. Plon, Chun-Hui Tsai, Tyler Reimschisel, Elizabeth Roeder, Amy D. Malphrus, Patricia A. Eng, Patricia Hixson, Sung-Hae L. Kang, Paweł Stankiewicz, Ankita Patel, Sau Wai Cheung	2010	83

About Ankita Patel

Ankita Patel is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 143 papers that have together received 6.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (81 papers), Prenatal Screening and Diagnostics (35 papers), Chromosomal and Genetic Variations (30 papers), Congenital heart defects research (26 papers), Genomics and Rare Diseases (19 papers), Genetics and Neurodevelopmental Disorders (17 papers), Acute Myeloid Leukemia Research (6 papers) and Fetal and Pediatric Neurological Disorders (6 papers). The work is most often cited by research in Genetics (4.1k citations), Pediatrics, Perinatology and Child Health (1.7k citations), Molecular Biology (2.8k citations), Genetics (324 citations) and Rheumatology (453 citations). Ankita Patel has collaborated with scholars based in United States, India and Canada. Frequent co-authors include Sau Wai Cheung, James R. Lupski, Chad A. Shaw, Paweł Stankiewicz, Arthur L. Beaudet, Carlos A. Bacino, A. Craig Chinault, Constance A. Griffin, Elizabeth J. Perlman and Cheryl M. Coffin. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Prenatal Diagnosis, PLoS Genetics and American Journal of Medical Genetics Part A.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Ankita Patel

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